5-''O''-Methylmyricetin

5-O-Methylmyricetin
Names
	IUPAC name 3,7-dihydroxy-5-methoxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
	Other names 5-Methylmyricetin
Identifiers
3D model (JSmol)	Interactive image; Interactive image;
ChemSpider	4477964 ;
PubChem CID	5319731;
	InChI InChI=1S/C16H12O8/c1-23-10-4-7(17)5-11-12(10)14(21)15(22)16(24-11)6-2-8(18)13(20)9(19)3-6/h2-5,17-20,22H,1H3 Key: DDVGNSDGGWHPQZ-UHFFFAOYSA-N ; InChI=1/C16H12O8/c1-23-10-4-7(17)5-11-12(10)14(21)15(22)16(24-11)6-2-8(18)13(20)9(19)3-6/h2-5,17-20,22H,1H3 Key: DDVGNSDGGWHPQZ-UHFFFAOYAT;
	SMILES COC1=C2C(=CC(=C1)O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O; O=C1c3c(O/C(=C1/O)c2cc(O)c(O)c(O)c2)cc(O)cc3OC;
Properties
Chemical formula	C16H12O8
Molar mass	332.26 g/mol
Density	1.731 g/mL
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

5-O-Methylmyricetin is an O-methylated flavonol, a type of flavonoid. It is the 5-O-methyl derivative of myricetin.

It occurs naturally and can also be synthetized.^[1]

References

↑ P. N. Sarma, G. Srimannarayana and N. V. Subba Rao (1974). "Synthesis of naturally occurring partial methyl ethers of myricetin". Proceedings Mathematical Sciences. 80 (4).

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.